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dc.contributor.authorSchulz, Eilien
dc.contributor.authorKaragianni, Anna
dc.contributor.authorKoch, Marcus
dc.contributor.authorFuhrmann, Gregor
dc.date.accessioned2020-01-03T14:06:40Z
dc.date.available2020-01-03T14:06:40Z
dc.date.issued2019-12-02
dc.identifier.citationEur J Pharm Biopharm. 2019 Dec 2. pii: S0939-6411(19)31309-8. doi: 10.1016/j.ejpb.2019.11.010.en_US
dc.identifier.issn1873-3441
dc.identifier.pmid31805356
dc.identifier.doi10.1016/j.ejpb.2019.11.010
dc.identifier.urihttp://hdl.handle.net/10033/622060
dc.description.abstractIn recent years, extracellular vesicles (EVs) and outer membrane vesicles (OMVs) have become an extensive and diverse field of research. They hold potential as diagnostic markers, therapeutics and for fundamental biological understanding. Despite ongoing studies, numerous information regarding function, content and stability of EVs remains unclear. If EVs and OMVs ought to be used as therapeutics and in clinical environments, their stability is one of the most important factors to be considered. Especially for formulation development, EVs and OMVs need to be stable at higher temperatures. To the best of our knowledge, very little work has been published regarding heat stability of neither EVs nor OMVs. In the present study, we investigated B lymphoblastoid cell-derived EVs and OMVs derived from myxobacterial species Sorangiineae as model vesicles. We exposed the vesicles to 37 °C, 50 °C, 70 °C and 100 °C for 1 h, 6 h and 24 h, and also autoclaved them. Interestingly, physico-chemical analyses such as size, particle concentration and protein concentration showed minor alterations, particularly at 37 °C. Flow cytometry analysis emphasised these results suggesting that after heat impact, EVs and OMVs were still able to be taken up by macrophage-like dTHP-1 cells. These data indicate that both mammalian and bacterial vesicles show intrinsic stability at physiological temperature. Our findings are important to consider for vesicle formulation and for advanced bioengineering approaches.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectautoclavingen_US
dc.subjectdrug carriersen_US
dc.subjectextracellular vesiclesen_US
dc.subjectflow cytometryen_US
dc.subjectheat stabilityen_US
dc.subjectlymphoblastoid cellsen_US
dc.subjectmyxobacteriaen_US
dc.subjectouter membrane vesiclesen_US
dc.titleHot EVs - how temperature affects extracellular vesicles.en_US
dc.typeArticleen_US
dc.contributor.departmentHIPS, Helmholtz-Institut für Pharmazeutische Forschung Saarland, Universitätscampus E8.1 66123 Saarbrücken, Germany.en_US
dc.identifier.journalEuropean Journal of Pharmaceutics and Biopharmaceuticsen_US
dc.source.journaltitleEuropean journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-ShareAlike 4.0 International